Define the product
Fix the name, use, form, market and formulation version.
Collect evidence
Link raw-material SDSs, specifications, tests and measured properties.
Assess hazards
Apply the relevant CLP data hierarchy and methods.
Draft the sections
Feed all sixteen sections from one controlled data set.
Review and approve
Check units, cross-references, label elements and limitations.
Example workflow
For an acidic cleaner, link raw materials, concentration ranges, final pH and the classification rationale.
Checklist
Common mistakes
Frequently asked questions
Can software make every decision?
No. It can support the workflow, but evidence and competent review determine quality.
Should source records be retained?
Yes, so decisions and updates remain traceable.
Does a general answer validate a specific product?
No. The actual composition, form, supplier data and intended use must be assessed.
Who should approve the result?
A competent person should review the data, method and internal consistency before supply.
Primary sources
Check the current consolidated version and the exact substance or product scope before use.